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A Trial for a Personalized Medication Management Platform to Improve Medication Adherence

T

Taipei Medical University

Status

Completed

Conditions

Patients Take Medicine

Treatments

Device: Personalized Medication Management Platform for SMS Reminder

Study type

Interventional

Funder types

Other

Identifiers

NCT02197689
NSC 99-2218-E-038-001

Details and patient eligibility

About

Taiwan has attracted much attention for its National Health Insurance (NHI) and healthcare system around the world with many countries in Europe and the United States using it as a benchmark. However, increasing medication costs over the past two years account for more than 25% of total expenditure, surpassing every OECD member and mounting increasing pressure on the NHI. Nevertheless, patient medication adherence is relatively low. Thus, the investigators assessed the effectiveness of a personalized medication management system for improving the medication adherence for patients, in order to save long term medication costs.

Full description

Design, Setting and Patients: The investigators developed a mobile personalized medication management platform (PMMP) to reduce delayed and missed medications. The investigators conducted a randomized control trial in medical centers of northern Taiwan from January 2010 to July 2012 using 1198 participants that missed or delayed their medications during past three days. They received a minimum 7-day to 14-day maximum medication prescription.

Interventions: Patients were randomized into a control group which non-received any SMS reminder for medication using and an intervention group which received a SMS reminder everyday in mobile devices.

Primary Outcome(s) and Measure(s): The primary outcomes were compared patient medication adherence among experimental and control groups.

Enrollment

763 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Delayed or forgot to take medications over the last 3 days
  • Received a min. 7-day medication prescription
  • Able to receive SMS using mobile phones / devices
  • 20 years or older
  • Having intention to receive active treatment

Exclusion criteria

  • Unable to receive SMS via mobile phones
  • Illiterate and < 20 years of age
  • Received outpatient prescription drugs for ≤ 7 days
  • External use, injections and traditional Chinese medicine
  • Planned to go abroad
  • Cold, cough, or prescribed with analgesics

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

763 participants in 2 patient groups

SMS Medication Reminder
Experimental group
Description:
763 patients were assigned to experimental group
Treatment:
Device: Personalized Medication Management Platform for SMS Reminder
No SMS Reminder
No Intervention group
Description:
435 patients were assigned to control group as no SMS reminder

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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